A Case of Immunoglobulin G4-related Disease Complicated by Atopic Dermatitis Responsive to Upadacitinib Treatment.

JAK1 inhibition glucocorticoid resistance glucocorticoids immunoglobulin G4-related disease upadacitinib

Journal

Modern rheumatology case reports
ISSN: 2472-5625
Titre abrégé: Mod Rheumatol Case Rep
Pays: England
ID NLM: 101761026

Informations de publication

Date de publication:
23 Aug 2024
Historique:
received: 11 03 2024
revised: 04 04 2024
accepted: 14 08 2024
medline: 23 8 2024
pubmed: 23 8 2024
entrez: 23 8 2024
Statut: aheadofprint

Résumé

Immunoglobulin G4-related disease is mainly treated with glucocorticoids. In many cases, this disease is resistant to glucocorticoids, and their toxicity can be a problem. We encountered a patient with immunoglobulin G4-related disease affecting multiple organs (such as the skin, lung, and lacrimal gland), who had comorbidities, including atopic dermatitis and diabetes. In this case, while glucocorticoid tapering was difficult, the introduction of upadacitinib resulted in remission of both atopic dermatitis and immunoglobulin G4-related disease without glucocorticoid dose escalation. Peripheral blood flow cytometry analysis showed that the proportions of activated non Th1/Th17 cells subset (Th2 cells), follicular helper T cells, and plasmocytes were increased before upadacitinib therapy but all normalised after treatment. Interleukin-4 and interleukin-21 signals are important for the differentiation of CD4+ T cells into type 2 helper T or B cells in the peripheral blood. Our case suggested that inhibition of Janus kinase 1, which mediates these signals, might have contributed to improved pathological conditions in immunoglobulin G4-related disease.

Identifiants

pubmed: 39177378
pii: 7739790
doi: 10.1093/mrcr/rxae047
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Japan College of Rheumatology 2024. Published by Oxford University Press. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site–for further information please contact journals.permissions@oup.com.

Auteurs

Katsuhide Kusaka (K)

Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Fukuoka, Japan.

Shingo Nakayamada (S)

Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Fukuoka, Japan.

Kentaro Hanami (K)

Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Fukuoka, Japan.

Aya Nawata (A)

Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Fukuoka, Japan.

Yoshiya Tanaka (Y)

Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Fukuoka, Japan.

Classifications MeSH